Good Sense Nasal

Product NDC: 0113-0304
11-digit product format: 001130304
Labeler code: 0113
Product ID: 0113-0304_140a1a6e-2f5d-453b-b593-cd00fe83c1d2
Type: HUMAN OTC DRUG
Nonproprietary name: oxymetazoline hydrochloride
Dosage form: SPRAY
Route: NASAL
Labeler: L. Perrigo Company
Application: M012
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 1989-09-15
Substance: OXYMETAZOLINE HYDROCHLORIDE
Active strength: .5 mg/mL
Pharmacologic classes: Imidazolines [CS], Increased Sympathetic Activity [PE], Vasoconstriction [PE], Vasoconstrictor [EPC]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	0113-0304	0113-0304-72	D	Discontinued by firm		2026-10-21

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 11 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product: Yes
Brand name base: Good Sense Nasal
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
OXYMETAZOLINE HYDROCHLORIDE	.5 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
K89MJ0S5VY	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1000990	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
276d7d3c-c4a7-4754-8845-c38f85aac5f7	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
e67be450-f8e4-4bc1-88bd-1259d379f55f	Product name	1	20210127
c53f3286-4062-4cf5-8355-399519c639a6	Product name	1	20170424
a993dfc5-f219-4460-bde6-30dd724d9ef0	Product name	1	20160818
9869efd7-d6dd-0665-5b67-53adbe6ef15e	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
0113-0304-10	Good Sense Nasal	1 in 1 CARTON	SPRAY	1	9
0113-0304-10	Good Sense Nasal	30 mL in 1 BOTTLE, SPRAY	SPRAY	30	9
0113-0304-72	Good Sense Nasal	37 mL in 1 BOTTLE, SPRAY	SPRAY	37	9
0113-0304-72	Good Sense Nasal	1 in 1 CARTON	SPRAY	1	9

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0113-0304-10	ML - Milliliter	0113-0304	f827fba0-4894-429a-92d3-b24b42fd8aab	1	2012-07-24
0113-0304-72	ML - Milliliter	0113-0304	29a9f677-8f87-44c7-8c96-531d5824765e	1	2024-02-14

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
OXYMETAZOLINE HYDROCHLORIDE	ACTIVE INGREDIENT	K89MJ0S5VY	GOOD SENSE NASAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [L. PERRIGO COMPANY]	5
OXYMETAZOLINE	ACTIVE MOIETY	8VLN5B44ZY	GOOD SENSE NASAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [L. PERRIGO COMPANY]	5
BENZALKONIUM CHLORIDE	INACTIVE INGREDIENT	F5UM2KM3W7	GOOD SENSE NASAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [L. PERRIGO COMPANY]	5
BENZYL ALCOHOL	INACTIVE INGREDIENT	LKG8494WBH	GOOD SENSE NASAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [L. PERRIGO COMPANY]	5
EDETATE DISODIUM	INACTIVE INGREDIENT	7FLD91C86K	GOOD SENSE NASAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [L. PERRIGO COMPANY]	5
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	GOOD SENSE NASAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [L. PERRIGO COMPANY]	5
POVIDONES	INACTIVE INGREDIENT	FZ989GH94E	GOOD SENSE NASAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [L. PERRIGO COMPANY]	5
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	GOOD SENSE NASAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [L. PERRIGO COMPANY]	5
SODIUM PHOSPHATE, DIBASIC	INACTIVE INGREDIENT	GR686LBA74	GOOD SENSE NASAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [L. PERRIGO COMPANY]	5
SODIUM PHOSPHATE, MONOBASIC	INACTIVE INGREDIENT	3980JIH2SW	GOOD SENSE NASAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [L. PERRIGO COMPANY]	5
WATER	INACTIVE INGREDIENT	059QF0KO0R	GOOD SENSE NASAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [L. PERRIGO COMPANY]	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0113-0304	GOOD SENSE NASAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [L. PERRIGO COMPANY]	9	Current NDC, Legacy NDC, 4 package rows	20240912_276d7d3c-c4a7-4754-8845-c38f85aac5f7.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 98 of 180 · 3,583 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Childrens Giltuss Honey DM Cough	DEXTROMETHORPHAN HBR	Gil Pharmaceutical Corp	a8c5027f-9701-fb07-e053-2a95a90a6029	2025-10-09	Warnings	Exact identifier application number: M012
Childrens Giltuss Honey Cough and Chest Congestion	DEXTROMETHORPHAN HBR, GUAIFENESIN	Gil Pharmaceutical Corp	a8c052d8-fb9f-09f2-e053-2a95a90a37af	2025-10-09	Warnings	Exact identifier application number: M012
Giltuss EX Expectorant	GUAIFENESIN	Gil Pharmaceutical Corp	a8c53c14-ba82-2c68-e053-2a95a90a9894	2025-10-09	Warnings	Exact identifier application number: M012
Giltuss Severe Sinus	OXYMETAZOLINE HCL	Gil Pharmaceutical Corp	ab7fae3b-1f7d-5d0f-e053-2a95a90a148e	2025-10-09	Warnings	Exact identifier application number: M012
Giltuss Honey DM Cough	DEXTROMETHORPHAN HBR	Gil Pharmaceutical Corp	a8c08532-1169-6603-e053-2a95a90a3484	2025-10-09	Warnings	Exact identifier application number: M012
Childrens Giltuss EX Expectorant	GUAIFENESIN	Gil Pharmaceutical Corp	a8c59e6d-c11c-2664-e053-2a95a90a8333	2025-10-09	Warnings	Exact identifier application number: M012
GILTUSS DIABETIC DM	DEXTROMETHORPHAN HBR	Gil Pharmaceutical Corp	bd367ce1-996b-45bc-865e-b6aafe0ea7b0	2025-10-09	Warnings	Exact identifier application number: M012
Giltuss DM	DEXTROMETHORPHAN HBR	Gil Pharmaceutical Corp	1a4fe686-3085-4543-bd6c-f20580b1df50	2025-10-09	Warnings	Exact identifier application number: M012
Giltuss D Allergy and Congestion	CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HCL	Gil Pharmaceutical Corp	8591003c-c2ec-df65-e053-2a91aa0a42fb	2025-10-09	Warnings	Exact identifier application number: M012
Gilphex	GUAIFENESIN, PHENYLEPHRINE HCL	Gil Pharmaceutical Corp.	e7c8fb97-02cf-4df6-b477-9ff69d6b675d	2025-10-09	Warnings	Exact identifier application number: M012
Childrens Allergy Relief	DIPHENHYDRAMINE HCL	Rite Aid Corporation	d9f26677-ddef-4098-b564-9aa5734e088b	2025-10-09	Warnings	Exact identifier application number: M012
Kalaya Breathe Easy Vaporizing Rub	VAPORIZING RUB	Avaria Health & Beauty Corp	7adf96b1-03af-a87b-e053-2a91aa0a4585	2025-10-08	Warnings	Exact identifier application number: M012
Equate Rub	CAMPHOR, EUCALYPTUS OIL, MENTHOL	Walmart Inc	01e1f418-c232-e89e-e063-6294a90abd35	2025-10-08	Warnings	Exact identifier application number: M012
Equate	OXYMETAZOLINE HCL	Walmart Inc	020942b1-59d4-a19d-e063-6394a90a5d87	2025-10-08	Warnings	Exact identifier application number: M012
Cough Drops Dollar General Assorted Flavors 80ct	MENTHOL	Dollar General	425d2e63-f5bc-45fb-b330-967ae64cfddb	2025-10-08	Warnings	Exact identifier application number: M012
Cough Drops Dollar General Cherry 200ct	MENTHOL	Dollar General Corporation	a17aece2-abd8-452a-9da8-2e303845900b	2025-10-08	Warnings	Exact identifier application number: M012
Cough Drops Dollar General Cherry 30ct	MENTHOL	Dollar General Corporation	b96268da-d6f2-41e4-ba04-ce419376f626	2025-10-08	Warnings	Exact identifier application number: M012
Cough Drops Dollar General Cherry 30ct	MENTHOL	Dollar General Corporation	51ccf39a-ae9b-4e6a-856c-002c296f5d07	2025-10-08	Warnings	Exact identifier application number: M012
Cough Drops Dollar General Honey Lemon 200ct	MENTHOL	Dollar General Corporation	8f8a9474-f388-4ede-85f2-86222b15ee58	2025-10-08	Warnings	Exact identifier application number: M012
Cough Drops Dollar General Honey Lemon 200ct	MENTHOL	Dollar General Corporation	f85f1a15-db7f-4bb5-9313-24702660054e	2025-10-08	Warnings	Exact identifier application number: M012

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
K89MJ0S5VY	OXYMETAZOLINE HYDROCHLORIDE	2315-02-8	OXYMETAZOLINE HYDROCHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1000990	oxymetazoline HCl 0.05 % Nasal Spray	PSN	276d7d3c-c4a7-4754-8845-c38f85aac5f7	9
1000990	oxymetazoline hydrochloride 0.5 MG/ML Nasal Spray	SCD	276d7d3c-c4a7-4754-8845-c38f85aac5f7	9
1000990	oxymetazoline hydrochloride 0.05 % Nasal Spray	SY	276d7d3c-c4a7-4754-8845-c38f85aac5f7	9
1000990	oxymetazoline HCl 0.05 % Nasal Spray	PSN	b6fbc0ba-7e88-4ab9-b0fa-1e1e8f9132fe	1
1000990	oxymetazoline HCl 0.05 % Nasal Spray	PSN	f91b7c1f-e074-4767-b9c8-dbf1937a6a0f	1
1000990	oxymetazoline hydrochloride 0.5 MG/ML Nasal Spray	SCD	b6fbc0ba-7e88-4ab9-b0fa-1e1e8f9132fe	1
1000990	oxymetazoline hydrochloride 0.5 MG/ML Nasal Spray	SCD	f91b7c1f-e074-4767-b9c8-dbf1937a6a0f	1
1000990	oxymetazoline hydrochloride 0.05 % Nasal Spray	SY	b6fbc0ba-7e88-4ab9-b0fa-1e1e8f9132fe	1
1000990	oxymetazoline hydrochloride 0.05 % Nasal Spray	SY	f91b7c1f-e074-4767-b9c8-dbf1937a6a0f	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
0113-0304-10	00113030410	1 BOTTLE, SPRAY in 1 CARTON (0113-0304-10) / 30 mL in 1 BOTTLE, SPRAY	1989-09-15	0000-00-00	No	No	Current
0113-0304-72	00113030472	1 BOTTLE, SPRAY in 1 CARTON (0113-0304-72) > 37 mL in 1 BOTTLE, SPRAY	1989-09-15	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Perrigo Nasal Spray Drug Facts	Sportpharm LLC	2026-02-06	HUMAN OTC DRUG LABEL	1
Perrigo Nasal Spray Drug Facts	A-S Medication Solutions	2024-10-31	HUMAN OTC DRUG LABEL	1
Perrigo Nasal Spray Drug Facts	L. Perrigo Company	2024-09-08	HUMAN OTC DRUG LABEL	9